Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs61734270
rs61734270
PTGIS
1.000 0.040 20 49524089 missense variant C/T snv 9.8E-04 9.6E-04
CUI: C0036346
Disease: Schizophrenia, Childhood
Schizophrenia, Childhood 		0.700 1.000 1 2016 2016